跳至主要内容
临床试验/NCT07624175
NCT07624175已完成2 期

Immunogenicity and Tolerability of Typhoid Conjugate Vaccine (TCV) 5-6 Years After Routine Vaccines Administered With or Without TCV Among Children Younger Than 2 Years in Ouagadougou, Burkina Faso

Kathleen Neuzil1 个研究点 分布在 1 个国家目标入组 147 人开始时间: 2024年8月17日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
147
试验地点
1

研究概览

简要总结

This study evaluated the persistence of immunity following primary typhoid conjugate vaccination in early childhood and assessed the immunogenicity and safety of a booster dose administered 5-6 years later. Children previously enrolled in a Phase 2 randomized clinical trial of Vi-tetanus toxoid conjugate vaccine (Vi-TT) were re-enrolled at 6-7 years of age. Participants who previously received Vi-TT received a booster dose of Vi-CRM, while control participants received their first TCV dose.

Anti-Vi IgG antibody responses were measured at baseline and 28 days post-vaccination. Safety was assessed through solicited and unsolicited adverse events. This study provides data on durability of TCV immunity and the potential role of booster dosing in endemic settings.

详细描述

This prospective, open-label interventional study followed children previously enrolled in a Phase 2 randomized controlled trial of Vi-TT administered in infancy. Approximately 5-6 years later, participants were re-contacted and assigned to receive either a booster TCV dose (Vi-CRM) or a first TCV dose depending on prior vaccination status.

Immunogenicity was assessed using anti-Vi IgG ELISA assays at baseline and 28 days post-vaccination. Safety outcomes included solicited and unsolicited adverse events and serious adverse events. The study was conducted at a single clinical site in Ouagadougou, Burkina Faso.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
6 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Male or female children previously enrolled in the 2018-2019 Phase 2 typhoid conjugate vaccine trial
  • Residence within study area
  • Parent/guardian provides informed consent

排除标准

  • Receipt of blood products within 6 months
  • Prior typhoid conjugate vaccine receipt outside the study
  • Medical condition interfering with evaluation
  • Acute illness or fever prior to vaccination (temporary exclusion)

研究者

发起方
Kathleen Neuzil
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Kathleen Neuzil

Professor

University of Maryland, Baltimore

研究点 (1)

Loading locations...

相似试验